Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population

Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample

(2009) ML Mostacciuolo et al.   CLINICAL GENETICS

165th ENMC International Workshop: Distal myopathies 6–8th February 2009 Naarden, The Netherlands

(2009) B. Udd   NEUROMUSCULAR DISORDERS

Estimating the prevalence of polymyositis and dermatomyositis from administrative data: age, sex and regional differences

(2008) S Bernatsky et al.   ANNALS OF THE RHEUMATIC DISEASES

Myofibrillar myopathies

(2008) Duygu Selcen   CURRENT OPINION IN NEUROLOGY

cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark

(2008) Morten Duno et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

156th ENMC International Workshop: Desmin and protein aggregate myopathies, 9–11 November 2007, Naarden, The Netherlands

(2008) Hans H. Goebel et al.   NEUROMUSCULAR DISORDERS

Gene table of monogenic neuromuscular disorders (nuclear genome only)

(2008)   NEUROMUSCULAR DISORDERS

Muscular dystrophies due to glycosylation defects

(2008) Francesco Muntoni et al.   Neurotherapeutics

Prevalence of mitochondrial DNA disease in adults

(2007) Andrew M. Schaefer et al.   ANNALS OF NEUROLOGY

Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients

(2007) Michela Guglieri et al.   HUMAN MUTATION